LivingGLP1
Descriptive only

Kidney composite with 40 percent eGFR decline

Type 2 diabetes (adults)

longest follow-upCause specific hazardsDoses of a drug pooledHazard ratio
1
Randomized trials
2
Treatments
0
Participants
2
Trial arms

In plain language

No network meta-analysis was fitted here. The protocol requires at least two trials forming a connected network; this outcome has 1 trial. The trial data below are shown as reported.

Network of trials

Each circle is a treatment; each line joins treatments that were randomized against each other in at least one trial.
EXENER_SCPLACEBO
Node area shows participants; line width shows trials comparing two treatments directly. Blue: GLP-1 receptor agonist containing treatments; grey: comparators. Hover over or tab to a node or line for details.

Baseline characteristics of the trials

The baseline value of each effect modifier or prognostic factor that applies here, per trial: mean or percent over arms, weighted by the number randomized. A note under a value names a stand in (a median for a mean, 100 minus the male share, Asian subgroup rows, an all Asian site list); "not reported" means no source of the trial prints it.
Baseline effect modifiers and prognostic factors per trial
TrialKidney function (eGFR) (mL/min/1.73 m2)
prognostic factor, effect modifier; 1 of 1
Albuminuria (mg/g)
prognostic factor; 1 of 1
NCT01144338
S000905
76.8523.35

Comparability of the trials

Checked across designs (the set of treatments each trial compares) for eligibility, outcome definition and assessment, and the baseline factors above. Flags point to possible intransitivity; notes describe variation that is not tied to design.

No comparability concerns were found.

Comparability items per trial
Trialtime weeksanalysis setdefinitioninstrumentadjudicatedproportion methodintercurrent events (discontinuation)intercurrent events (rescue)blindingfundingstart yearEligibility
NCT01144338391.35randomizedSustained 40 percent eGFR decline or ESRD (chronic dialysis or transplant)not statednot statednot statednot statednot stateddouble_blindindustry2010age 18 or older; HbA1c 6.5 to 10.0 percent; eGFR 30 or more

Trial data

What each trial contributes. Arm rows give the arm value with its standard error, or events over participants; contrast rows give the hazard ratio on the analysis scale (log) against the trial's first row. Flags mark converted, combined or approximated inputs.
Trial data entering this analysis
TrialArmTreatmentWeekDataValueSEEvents / NFlagsSource
NCT01144338A1PLACEBO391.35contrast, hrR0025168:Results
NCT01144338A2EXENER_SC391.35contrast, hr-0.1510.094R0025168:Results

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